Welcome to LookChem.com Sign In|Join Free

CAS

  • or

109922-57-8

Post Buying Request

109922-57-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

109922-57-8 Usage

General Description

Quinoline-4-acetic acid is a chemical compound with the formula C10H7NO2. It is a derivative of quinoline, a heterocyclic compound consisting of a benzene ring fused to a pyridine ring. Quinoline-4-aceticacid is used in the pharmaceutical industry as a starting material in the synthesis of various drugs, including anti-inflammatory and anti-tumor agents. Quinoline-4-acetic acid is also used in the production of dyes and pigments. It is a versatile and important building block in organic synthesis, and its unique structure and properties make it valuable in a variety of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 109922-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,2 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 109922-57:
(8*1)+(7*0)+(6*9)+(5*9)+(4*2)+(3*2)+(2*5)+(1*7)=138
138 % 10 = 8
So 109922-57-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c13-11(14)7-8-5-6-12-10-4-2-1-3-9(8)10/h1-6H,7H2,(H,13,14)

109922-57-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-quinolin-4-ylacetic acid

1.2 Other means of identification

Product number -
Other names [4]Chinolyl-essigsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:109922-57-8 SDS

109922-57-8Relevant articles and documents

STEREOSPECIFIC SYNTHESIS OF ERYTHRO CINCHONA ALKALOIDS FROM SECOLOGANIN

Brown, Richard T.,Curless, Dale

, p. 6005 - 6008 (1986)

A short, diastereoselective synthesis of (+)-dihydrocinchonine (7) and (-)-dihydrocinchonidine (8) from their biogenetic precursor, secologanin (1a), and lepidine has been achieved in 28percent overall yield.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 109922-57-8